NDC 42708-202
Metformin Hydrochloride 1000 mg tablet, film coated
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-932.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Harman Finochem Limited | Chhatrapati Sambhajinagar, India | Makes it | No problems foundFeb 23, 2024 · 1 inspection |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Metformin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 1000 mg
- Approval
- ANDA ANDA213320
- On the market since
- Aug 25, 2025
- Package NDCs
42708-202-30- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2026
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